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Calcitriol and Gefitinib With or Without Dexamethasone in Treating Patients With Advanced Solid Tumors

10. januar 2014 oppdatert av: Roswell Park Cancer Institute

A Phase I Study of Intravenous (IV) Calcitriol in Combination With ZD1839 (IRESSA®) in Refractory Solid Tumors

RATIONALE: Gefitinib may stop the growth of tumor cells by blocking the enzymes necessary for their growth. Calcitriol may help tumor cells develop into normal cells. Dexamethasone may increase the effectiveness and decrease the side effects of gefitinib and calcitriol.

PURPOSE: This phase I trial is studying the side effects and best dose of calcitriol when given together with gefitinib or when given together with gefitinib and dexamethasone in treating patients with advanced solid tumors.

Studieoversikt

Detaljert beskrivelse

OBJECTIVES:

Primary

  • Determine the maximum tolerated dose (MTD), toxic effects, and tolerability of calcitriol alone and in combination with gefitinib with or without dexamethasone in patients with advanced solid tumors.

Secondary

  • Determine the pharmacokinetics and pharmacodynamics of these regimens in these patients.
  • Determine any tumor responses in patients treated with these regimens.

OUTLINE: This is a dose-escalation study of calcitriol.

  • Stage 1: Patients receive calcitriol IV over 1 hour on days 1, 15, and 22 and oral gefitinib once daily on days 8-28 during course 1. For all subsequent courses, patients receive calcitriol IV over 1 hour on days 1, 8, 15, and 22 and oral gefitinib once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

Cohorts of 3-6 patients receive escalating doses of calcitriol with a fixed dose of gefitinib until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.

  • Stage 2: Patients receive calcitriol (beginning at 1 dose level below the MTD determined in stage 1) and gefitinib as in stage 1. Patients also receive oral dexamethasone once on the day before and twice on the day of each dose of calcitriol.

Cohorts 3-6 patients receive escalating doses of calcitriol with fixed doses of gefitinib and dexamethasone until the MTD is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.

PROJECTED ACCRUAL: A total of 21-36 patients will be accrued for this study within 1 year.

Studietype

Intervensjonell

Registrering (Faktiske)

53

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • New York
      • Buffalo, New York, Forente stater, 14263-0001
        • Roswell Park Cancer Institute

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

DISEASE CHARACTERISTICS:

  • Histologically confirmed advanced solid tumor

    • Metastatic or unresectable disease
    • Standard curative or palliative measures do not exist or are no longer effective
  • No known brain metastases

PATIENT CHARACTERISTICS:

Age

  • 18 and over

Performance status

  • ECOG 0-2 OR
  • Karnofsky 60-100%

Life expectancy

  • More than 3 months

Hematopoietic

  • WBC ≥ 3,000/mm^3
  • Hemoglobin ≥ 8 g/dL
  • Absolute neutrophil count ≥ 1,500/mm^3
  • Platelet count ≥ 100,000/mm^3

Hepatic

  • Bilirubin normal
  • AST and ALT ≤ 2.5 times upper limit of normal
  • No unstable or uncompensated hepatic disease

Renal

  • Creatinine normal OR
  • Creatinine clearance ≥ 60 mL/min
  • No prior hypercalcemia
  • No kidney, ureteral, or bladder stones within the past 10 years
  • No unstable or uncompensated renal disease

Cardiovascular

  • Ejection fraction ≥ 30%
  • No heart failure or significant heart disease
  • No significant arrhythmias
  • No myocardial infarction within the past 3 months
  • No unstable angina pectoris
  • No symptomatic congestive heart failure
  • No other unstable or uncompensated cardiac disease

Pulmonary

  • No evidence of clinically active interstitial lung disease

    • Chronic, stable, asymptomatic, radiographic changes allowed
  • No other unstable or uncompensated respiratory disease

Other

  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for 30 days after study treatment
  • Able to receive oral medication
  • Willing to have serial skin biopsies
  • No prior allergic reaction to compounds of similar chemical or biological composition to study drugs or other agents used in this study
  • No ongoing or active infection
  • No known severe hypersensitivity to gefitinib or any of its excipients
  • No psychiatric illness or social situation that would preclude study compliance
  • No other severe or uncontrolled systemic disease or concurrent illness that would preclude study participation
  • No other significant clinical disorder or laboratory finding that would preclude study participation

PRIOR CONCURRENT THERAPY:

Biologic therapy

  • No concurrent filgrastim (G-CSF) or sargramostim (GM-CSF)

Chemotherapy

  • More than 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin) and recovered

Endocrine therapy

  • No other concurrent systemic glucocorticoid therapy

Radiotherapy

  • More than 4 weeks since prior radiotherapy and recovered

Surgery

  • Recovered from prior major surgery
  • No prior nephrectomy

Other

  • Recovered from all prior anticancer therapy
  • More than 30 days since prior non-approved or investigational drugs
  • More than 7 days since prior thiazides
  • No concurrent administration of any of the following:

    • Combination antiretroviral therapy for HIV-positive patients
    • Phenytoin
    • Carbamazepine
    • Barbiturates
    • Rifampin
    • Phenobarbital
    • Hypericum perforatum (St. John's wort)
    • Calcium supplements
    • Thiazides
    • Digoxin
  • No other concurrent investigational or commercial anticancer agents or therapies

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag

Hva måler studien?

Primære resultatmål

Resultatmål
Maksimal tolerert dose

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Marwan Fakih, MD, Roswell Park Cancer Institute

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. november 2002

Primær fullføring (Faktiske)

1. oktober 2006

Studiet fullført (Faktiske)

1. mai 2007

Datoer for studieregistrering

Først innsendt

10. juni 2004

Først innsendt som oppfylte QC-kriteriene

10. juni 2004

Først lagt ut (Anslag)

11. juni 2004

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

13. januar 2014

Siste oppdatering sendt inn som oppfylte QC-kriteriene

10. januar 2014

Sist bekreftet

1. januar 2014

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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